Effect Mobility During Induction of Labor on Time to Delivery. A Randomized Controlled Trial
Not Applicable
- Conditions
- Labor Onset and Length Abnormalities
- Registration Number
- NCT03784092
- Lead Sponsor
- Wolfson Medical Center
- Brief Summary
this is a andomized controlled trial the evaluates the effect of enhanced mobility, controlled via electronic pedometers, during induction of labor by extra amniotic balloon on time to delivery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 224
Inclusion Criteria
- pregnant women
- low risk pregnancies
- singlelton
- vertex position
- undergoing labor induction with extra amniotic catheter
- no contraindication for enhanced mobility
Exclusion Criteria
- medical recommendation for limited mobility
- status post cesarean delivery
- twin pregnancy
- premature rupture of membranes
- severe preeclampsia
- maternal comorbidity
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method time to delivery labor ( catheter placement till delivery completion) time from extra amniotic catheter placement till delivery
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie enhanced mobility's impact on labor duration in NCT03784092?
How does electronic pedometer-guided mobility compare to standard bed rest during labor induction?
Are there specific biomarkers associated with successful labor outcomes in patients using pedometers for mobility tracking?
What adverse events are linked to increased mobility during extra amniotic balloon induction and how are they managed?
What combination therapies or alternative approaches to labor induction are being explored alongside mobility interventions?